HOYER GmbH
DE-MF-000007883 · Germany · Butzbach
HOYER GmbH is registered in the European database on medical devices as a manufacturer, with 431 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 431 |
|---|
Devices declared under this manufacturer
- 32-SaÜ-DRi Normalsitz 87cm
- 37-S Kopfstütze
- 39-C/oG Kombisitz
- 43-S/oG PAAR Toilettengurte
- 49-SKF Spezialsitz Gr.XL
- 49-Sa kurz Spezialsitz Gr.L
- 49-Sa l Spezialsitz Gr.L
- 51/80 Brustgurt 80cm
- 52-Sa Aufricht- und Ankleidegurt bis 100cm
- Deckenlift 72005/200
- Hebebügel, blau lang
- Sender Funksteuerung
Showing 12 of 431 declared devices.
Catalogue references include 71603, 72162, 91309, 91378, 91388, 91430.
European nomenclature codes declared: V0805038002, V08050302, V08050399, V0805030102, V08050303, V0805038001.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 431 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 431 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. HOYER GmbH was not found in either the U.S. or the Canadian register.